LSD-Pip
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LSD-Pip
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|---|---|
| Systematic (IUPAC) name | |
| (8β)-6-methyl-8-(piperidin-1-ylcarbonyl)-9,10-didehydroergoline | |
| Clinical data | |
| Pregnancy cat. | ? |
| Legal status | ? |
| Identifiers | |
| CAS number | 50485-23-9 |
| ATC code | ? |
| PubChem | CID 308707 |
| Chemical data | |
| Formula | C21H25N3O |
| Mol. mass | 335.442 g/mol |
| SMILES | eMolecules & PubChem |
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LSD-Pip is a compound from the ergoline family, related to LSD but with the N,N-diethyl substitution replaced by a piperidine group. It is more potent than the corresponding pyrrolidine and morpholine analogues (LPD-824 and LSM-775 respectively), but is still several times less potent than LSD as a 5-HT2A agonist.[1] Early studies suggested this compound to be inactive as a hallucinogen in humans,[2] though this does not seem to have been confirmed by any more recent work.
See also
References
- ^ Michael Robert Braden PhD. Towards a biophysical understanding of hallucinogen action. Purdue University 2007.
- ^ CERLETTI A, DOEPFNER W (January 1958). "Comparative study on the serotonin antagonism of amide derivatives of lysergic acid and of ergot alkaloids". The Journal of Pharmacology and Experimental Therapeutics 122 (1): 124–36. PMID 13502837.
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